EP1053268A1 - Elastomers from compositions comprising rigid thermoplastic polyurethane - Google Patents
Elastomers from compositions comprising rigid thermoplastic polyurethaneInfo
- Publication number
- EP1053268A1 EP1053268A1 EP99907364A EP99907364A EP1053268A1 EP 1053268 A1 EP1053268 A1 EP 1053268A1 EP 99907364 A EP99907364 A EP 99907364A EP 99907364 A EP99907364 A EP 99907364A EP 1053268 A1 EP1053268 A1 EP 1053268A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition according
- rubber
- thermoplastic polyurethane
- less
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/0895—Manufacture of polymers by continuous processes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/22—Thermoplastic resins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
- C08L2666/20—Macromolecular compounds having nitrogen in the main chain according to C08L75/00 - C08L79/00; Derivatives thereof
Definitions
- the present invention relates to elastomers and preferably thermoplastic elastomers (TPE's) and more specifically to thermoplastic elastomers produced from compositions comprising rubber-like materials and rigid thermoplastic polyurethane, wherein the rubber-like material phase is optionally vulcanised or optionally dynamically vulcanised.
- TPE's thermoplastic elastomers
- thermoplastic elastomers produced from compositions comprising rubber-like materials and rigid thermoplastic polyurethane wherein the rubber-like material phase is optionally vulcanised or optionally dynamically vulcanised.
- Thermoplastic elastomers are a class of materials which combine properties of vulcanised rubber with the processing properties of conventional thermoplastics. Examples of these materials are well known in the art. Usually they consist of block copolymers, which exhibit a multiphase microstructure. Best known examples are styrene-elastomer block copolymers like styrene-butadiene-styrene (SBS) or l5 styrene-isoprene-styrene (SIS). Other examples are polyamide-elastomer and poiyurethane-elastomer multiblock copolymers. For more examples see e.g. chapter 13 of "Science and Technology of Rubber", 2nd ed., J. E. Mark et al. eds., Academic Press, 1994.
- Thermoplastic elastomers can also be produced by blending hard thermoplastic material 20 with a rubber-like material.
- hard thermoplastic material 20 examples are natural rubber-polypropylene (NR-PP) blends (TPNR's) and EPDM-PP blends, often referred to as thermoplastic olefins (TPO's).
- NR-PP natural rubber-polypropylene
- TPNR's natural rubber-polypropylene
- TPO's thermoplastic olefins
- Thermoplastic Elastomers from Rubber-Plastic Blends DE and BHOWMICK eds., Ellis Horwood, 1990.
- thermoplastic vulcanizate TPV
- EA elastomeric alloy
- TPVs are based on ethylene propylene diene monomer rubber/polypropylene (EPDM/PP) dynamically vulcanized blends (see e.g. US-A 3758643, US-A 3806558).
- EPDM/PP ethylene propylene diene monomer rubber/polypropylene
- Thermoplastic polyurethanes or TPU's are thermoplastic elastomers consisting of soft segments and hard segments commonly produced from the reaction between macroglycols, diisocyanates and short chain diols. They exhibit elastomeric as well as thermoplastic properties and show two major glass transition temperatures T g h and T g s , corresponding to respectively the hard and the soft phases.
- T g s is lower than about -10°C and the T g h higher than 50°C.
- Blends of TPU's with other thermoplastics are well known in the art. E.g. blends of TPU with polyoxymethylene (POM), polyvinylchloride (PVC), styrene acrylonitrile (SAN) and acrylonitrile butadiene styrene (ABS) are of commercial importance.
- POM polyoxymethylene
- PVC polyvinylchloride
- SAN styrene acrylonitrile
- ABS acrylonitrile butadiene styrene
- thermoplastic polyurethane exists called rigid TPU or rTPU, which contains no or only small amounts of soft segments. These products show thermoplastic behaviour but no elastomeric behaviour and are glassy or (semi-)crystalline at ambient temperature. They usually exhibit no major glass transition temperature (T fl ) below room temperature.
- US-A 4376834 to Goldwasser et al. teaches high impact resistant rigid TPU based on an organic polyisocyanate, a chain extender and from about 2 to about 25% of an isocyanate-reactive material with a functionality of >1.9 and a molecular weight of about 500 to 20000 (soft segment). It is suggested that the material has a two-phase morphology and that the lowest T g occurs below room temperature, while the T g of the urethane glass phase occurs at approximately 100°C.
- US-A 4567236 (to Goldwasser) teaches virtually the same rigid TPU which has only one T g which is claimed to be >50°C.
- the rigid TPU in US-A 4567236 is blended with materials known in the art as impact modifiers like ABS, ethylene vinyl acetate (EVA), chlorinated polyethylene (cPE), methylmethacrylate-butadiene-styrene and the like.
- the amount of impact modifier is said to range between 3 and 25% by weight. In the examples the amount of impact modifier used is 15 parts by weight on 85 parts by weight of rTPU.
- US-A 4822827 (to Beck et al.) teaches an improvement over the prior art rTPU's by replacing part of the chain extender composition with a cycloalkanediol.
- the novel rTPU's are characterised by a T g >125°C.
- US-A 5167899 (to Jezic) teaches the production of microfibers from rigid TPU's.
- An example is given of microfibers from a commercial rTPU ('ISOPLAST 301 , 'ISOPLAST' is a Trademark of DOW Chemical Co.) which composition matches this described in US-A 4822827.
- WO-A 93/02238 (to Moses et al.) teaches blends of PET and rTPU.
- the amount of polyol in the rTPU is limited in such a way that the T g remains >60°C.
- the rTPU used in the examples is again 'ISOPLAST 301 , however the T g is said to be 114°C.
- thermoplastic polymer blends having a Shore A hardness of about 55 to 70 comprising, in a volume percentage ratio of about 30:70 to 40:60, a PU component containing at least about 50 wt% polyisocyanate and a nitrile rubber component containing about 34 mol% acrylonitrile.
- thermoplastic elastomers Although numerous types of thermoplastic elastomers are known, there is still a need for improved thermoplastic materials having elastomeric properties.
- thermoplastic elastomers with useful properties can be produced by melt blending rigid TPU not having a major T g of less than 60°C and a rubber-like material having a T g of less than 20°C, the weight ratio of the rigid TPU and the rubber-like material being at most 85:15.
- TPU elastomers and of the rubber-like materials used. Because of the large number of possible combinations a wide range of materials can be produced with a wide range of properties.
- the invention thus relates to a composition
- a composition comprising (A) a rigid thermoplastic polyurethane not having a major T g of less than 60°C and (B) a rubber-like material having a T g of less than 20°C, wherein the weight ratio (A):(B) is at most 85:15.
- the rigid thermoplastic polyurethane (rTPU) of the present invention is obtainable by reaction of diisocyanate(s) with chain extender(s) and optionally macroglycol(s) at an isocyanate index of 95 to 105, pref. 98 to 102.
- thermoplastic polyurethanes may also be obtained by blending different polyurethanes in such amounts that the blend does not have a major T g of less than 60°C.
- isocyanate index is the ratio of isocyanate-groups over isocyanate-reactive hydrogen atoms present in a formulation, given as a percentage.
- the isocyanate index expresses the percentage of isocyanate actually used in a formulation with respect to the amount of isocyanate theoretically required for reacting with the amount of isocyanate-reactive hydrogen used in a formulation.
- the isocyanate index as used herein is considered from the point of view of the actual polymer forming process involving the isocyanate ingredient and the isocyanate-reactive ingredients. Any isocyanate groups consumed in a preliminary step to produce modified polyisocyanates (including such isocyanate-derivatives referred to in the art as quasi- or semi-prepolymers) or any active hydrogens reacted with isocyanate to produce modified polyols or polyamines, are not taken into account in the calculation of the isocyanate index. Only the free isocyanate groups and the free isocyanate-reactive hydrogens present at the actual elastomer forming stage are taken into account.
- the rTPU can be produced in the so-called one-shot, semi-prepolymer or prepolymer method, by casting, extrusion or any other process known to the person skilled in the art.
- the macroglycol optionally used has a molecular weight of between 500 and 20000 and 5 is used in an amount of 0 to 50% by weight, preferably less than 25% by weight, more preferably less than 10% by weight and most preferably less than 5% by weight, based on the total weight of the thermoplastic polyurethane.
- the macrodiol is always present in such an amount and composition that the rTPU does not have a major glass transition temperature below 60°C.
- the amount of macroglycols as a percentage of the total composition of the rigid TPU is defined as the softblock content of the rTPU.
- the macroglycols may be selected from polyesteramides, polythioethers, polycarbonates, polyacetals, polyolefins, polysiioxanes and, especially, polyesters and polyethers.
- Polyether glycols which may be used include products obtained by the polymerisation of a cyclic oxide, for example ethylene oxide, propylene oxide, butylene oxide or tetrahydrofuran in the presence, where necessary, of difunctional initiators.
- Suitable initiator compounds contain 2 active hydrogen atoms and include water, butanediol, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol and dipropylene glycol. Mixtures of initiators and/or cyclic oxides may be used.
- Especially useful polyether glycols include polyoxypropylene glycols and poly(oxyethylene-oxypropylene) glycols obtained by the simultaneous or sequential addition of ethylene or propylene oxides to difunctional initiators as fully described in the prior art. Random copolymers having oxyethylene contents of 10-80%, block copolymers having oxyethylene contents of up to 25% and random/block copolymers having oxyethylene contents of up to 50%, based on the total weight of oxyalkylene units, may be mentioned, in particular those having at least part of the oxyethylene groups at the end of the polymer chain.
- Other useful polyether glycols include polytetramethylene glycols obtained by the polymerisation of tetrahydrofuran.
- Polyester glycols which may be used include hydroxyl-terminated reaction products of dihydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, 1 ,4-butanediol, neopentyl glycol or 1 ,6-hexanediol, or mixtures of such dihydric alcohols, and dicarboxylic acids and their ester-forming derivatives, for example succinic, glutaric and adipic acids or their dimethyl esters, sebacic acid, phthalic anhydride, tetrachlorophthalic anhydride or dimethyl terephthalate or mixtures thereof.
- Polythioether glycols which may be used include products obtained by condensing thiodiglycol either alone or with other glycols, alkylene oxides or dicarboxylic acids.
- Polycarbonate glycols which may be used include products obtained by reacting diols such as 1,3-propanediol, 1 ,4-butanediol, 1 ,6-hexanediol, diethylene glycol or tetraethylene glycol with diaryl carbonates, for example diphenyl carbonate, or with phosgene.
- Polyacetal glycols which may be used include those prepared by reacting glycols such as diethylene glycol, triethylene glycol or hexanediol with formaldehyde. Suitable polyacetals may also be prepared by polymerising cyclic acetals.
- Suitable polyolefin glycols include hydroxy-terminated butadiene homo- and copolymers and suitable polysiioxane glycols include polydimethylsiloxane diols.
- Chain extenders can be any difunctional isocyanatereactive species with a molecular weight of less than 500, preferably a diol, more preferably a branched diol or blends of different types.
- Suitable chain extenders include aliphatic diols, such as ethylene glycol, 1 ,3-propanediol, 1 ,4-butanediol, 1 ,6-hexanediol, 1 ,2-propanediol, 1 ,3-butanediol, 2,3-butanediol, 1 ,3-pentanediol, 1 ,2-hexanediol, 3-methyl-1 ,5-pentanediol, diethylene glycol, dipropylene glycol and tripropylene glycol.
- aliphatic diols such as ethylene glycol, 1 ,3-propanediol, 1 ,4-butanediol, 1 ,6-hexanediol, 1 ,2-propanediol, 1 ,3-butanediol, 2,3-butanediol, 1
- Chain extenders with an odd-number of carbon atoms between the hydroxyl groups and chain extenders with a branched chain stucture like 2-methyl-1 ,3-propanediol, 2,2-dimethyl-2,3-propanediol, 1 ,3-propanediol, 1 ,5-pentanediol are preferred.
- Preferred chain extenders are neopentylglycol, 1,3-propanediol, 2-methyl-1 ,3-propanediol and other diols having a molecular weight of less than 500 containing an alkylene group with an odd number of carbon atoms between the two hydroxyl groups.
- Organic polyisocyanates may be selected from aliphatic, cycloaliphatic and araliphatic polyisocyanates, especially diisocyanates, like hexamethylene diisocyanate, isophorone 7 diisocyanate, cyclohexane-1 ,4-diisocyanate, 4,4'-dicyclohexylmethane diisocyanate and m- and p-tetramethylxylylene diisocyanate, and in particular aromatic polyisocyanates like tolylene diisocyanates (TDI), phenylene diisocyanates and most preferably diphenylmethane diisocyanates (MDI), particularly MDI comprising 4,4'-diphenylmethane diisocyanate.
- diisocyanates like hexamethylene diisocyanate, isophorone 7 diisocyanate, cyclohexane-1 ,4-diisocyanate, 4,4'-dicyclohex
- the diphenylmethane diisocyanates may consist essentially of pure
- the polyisocyanate component may also be an MDI-variant derived from a polyisocyanate composition containing at least 85% by weight of 4,4'-diphenylmethane diisocyanate.
- MDI variants are well known in the art and, for use in accordance with the invention, perticularly include liquid products obtained by introducing carbodiimide groups into said polyisocyanate composition and/or by reacting with one or more polyols.
- polyisocyanate compositions containing at least 90% by weight of 4,4'-diphenylmethane diisocyanate are preferred.
- Polyisocyanate compositions containing at least 95% by weight of 4,4'-diphenylmethane diisocyanate are most preferred.
- the rubber-like material used in the invention can be any conventional rubber known in the art having a T g of less than 20°C : non polar rubbers like butadiene rubber (BR), styrene butadiene rubber (SBR), isoprene rubber (IR), natural rubber (NR), butyl rubber (MR), ethylene propylene rubber (EPR), ethylene propylene diene monomer rubber (EPDM) and polar rubbers like nitrile rubber (NBR), carboxylated nitrile rubber (XNBR), acrylate rubber (ACM), chloroprene rubber(CR), ethylene acrylate rubber (EAM), nitrile-isoprene rubber (NIR), epichlorohydrin rubber (ECO) or halobutyl rubber.
- non polar rubbers like butadiene rubber (BR), styrene butadiene rubber (SBR), isoprene rubber (IR), natural rubber (NR), butyl rubber (MR), ethylene propylene rubber
- the rubber-like material used in the invention may also be thermoplastic elastomers (TPE's) like SBS, SIS, SEBS, TPU and the like, thermoplastic vulcanizates (TPVs) like ethylene propylene diene monomer rubber/polypropylene (EPDM/PP) dynamically vulcanized blends, plastomers like ethylene vinylacetate (EVA) copolymers or very low density polyethylene (VLDPE), or any thermoplastic elastomer derived from blends of plastics and rubbers.
- TPE's thermoplastic elastomers
- TPVs thermoplastic vulcanizates
- EPDM/PP ethylene propylene diene monomer rubber/polypropylene
- plastomers like ethylene vinylacetate (EVA) copolymers or very low density polyethylene (VLDPE), or any thermoplastic elastomer derived from blends of plastics and rubbers.
- a preferred rubber-like material is any material other than a polyurethane. More preferred are diene rubbers, hydrogenated diene rubbers, rubbers based on ethylene 8 propylene blends, nitrile rubbers or copolymers like EPR and EPDM rubbers.
- the rubber-like material has a T g below 0°C, more preferably below -20°C.
- the weight ratio rigid TPU:rubber-like material in the compositions of the present invention is at most 85:15, preferably at most 75:25 and more preferably at most 50:50.
- properties of the compositions of the invention may be improved through the use of compatibilizing agents.
- compatibilizing additives also called compatibilizers.
- Compounds of this kind are well known in the art and often are block copolymers or graft copolymers where the blocks consist of the same polymers which have to be compatibilized.
- the compatibilizers can be produced seperately and added before or after blending, or can be produced in-situ during blending. The latter process is referred to as reactive compatibilization.
- An overview of polymer compatibilization and examples of compatibilizers for different polymer pairs are given in "Polymer Blends and Alloys", Folkes and Hope Eds., Chapman &Hall, (1993).
- Compatibilizers useful in the invention can be non-reactive copolymers or non-reactive graft copolymers consisting of e.g. polyurethane-rubber graft copolymer, or a block copolymer where one block is compatible with the rTPU phase and the other block with the rubber-like material phase.
- reactive compatibilizers e.g. where all or part of the PU phase is modified to become reactive with the rubber-like material phase, or all or part of the rubber-like material phase is modified to become reactive with the PU phase, or both, can also be contemplated.
- the rubber-like material phase is vulcanized, preferably dynamically vulcanized, i.e. vulcanized during the blending process.
- Vulcanization of the rubber-like material phase can be achieved with compositions known to people skilled in the art. Sulphur systems, accelerated sulfur systems, peroxides, phenolics and the like are preferred vulcanizing systems. An overview of the most commonly used vulcanization systems can be found in " Science and Technology of Rubber", 2nd. Ed. academic press, 1994
- the rubber-like material phase may also be vulcanized in a conventional (i.e. non-dynamic) way, e.g. in a press mould.
- the polymer composition must therefore be 9 compounded with vulcanizing agents after which the material is compression moulded at higher temperatures to get formed and vulcanized.
- Melt blending and dynamic vulcanization can be achieved using conventional internal or external mixers well known in the art.
- blending can be achieved using e.g. a twin screw extruder, or a compounding single screw extruder.
- An overview of the practical aspects of polymer blending can be found in " Polymer Blends and Alloys", Folkes and Hope eds.Chapman & Hall, (1993).
- auxiliaries and additives typical for both polyurethanes and rubber technologies may be used as well.
- Additives and auxiliaries can be added to either or both of the TPU and the rubber-like material phase before, during or after blending and/or vulcanization.
- auxiliaries and additives include catalysts, for example tertiary amines and tin compounds, surface-active agents, for example siloxane-oxyalkylene copolymers, extender oils, flame retardants, plasticizers, organic and inorganic fillers, pigments, anti-oxidants, UV stabilizers, physical or chemical blowing agents, antireversion agents and internal mould release agents.
- the invention also relates to a process for preparing elastomers by melt-blending a rigid thermoplastic polyurethane which does not exhibit a major T g below 60°C, with a rubber-like material having a T g of less than 20°C, the weight ratio of the rigid thermoplastic polyurethane and the rubber-like material being at most 85:15, and to elastomers, preferably thermoplastic elastomers, thus obtained.
- compositions of the present invention are preferably in the form of a blend comprising (A) and (B), either liquid or solid.
- a particularly preferred form for the composition is a granular solid.
- compositions as herein described for making elastomers wherein (A) and (B) are mixed prior to or during the elastomer production.
- the elastomers of the invention combine some of the advantages of conventional TPU elastomers and of the rubber-like materials used. Because of the large number of possible combinations a wide range of materials can be produced with a wide range of properties. 10
- the resulting elastomers can be used in a number of applications such as shoesoles, shoe-insoles, automotive parts (dashboards, window seals, bumperholders) or other applications like watch straps, tool grips or cable insulation.
- 4,4'-MDI was mixed with 2-methyt-1 ,3-propanedioi at an isocyanate index of 101 , using a Heydolph bench mixer at 3000rpm. Both chemicals were initially at a temperature of 5 50°C and the total amount of the composition was 250g. Mixing time was 2 minutes. The reacting mixture was then poured in an open aluminium mould, placed on a thermostatted hot plate, set at 120°C. The mould had first been treated with a proper release agent. The amount poured was such that the thickness of the cast remained ⁇ 5mm. After 1 hour the cast was taken from the mould and put in an oven at 100°C for 10 24 hours. After cooling the cast was shredded.
- the T g of the resulting rigid TPU was measured by DSC to be 115°C.
- the DSC equipment used was a METTLER type TA4000 equipped with a DSC30 measuring cell at a heating rate 30°C/minute.
- the dry mixture was melt-blended in a HAAKE RHEOMIX 3000 internal mixer.
- the mixing rate was set at 80rpm and the temperature setting was 185°C. After complete melting of the blend, mixing continued for 3 minutes, after which the mixture was 20 discharged cooled, and shredded.
- the shredded blend was extruded using a HAAKE RHEOMEX R254, L/D 25, single screw extruder, equipped with a conventional PE screw with a compression ratio of 1 :3, and a 3mm rod die. Properties were measured on the extruded rods using an Instron 4500, operating with a cross-head speed of 100mm/min. The resulting material showed 25 a stress at break of 1.3MPa and and elongation at break of 90%. The shore A hardness was about 70. 12
- Example 2 Example 2
- 100g of the shredded TPU of example 1 was dry-blended with 150g nitrile rubber of example 1.
- the dry mixture was melt-blended in a HAAKE RHEOMIX 3000 internal mixer.
- the mixing rate was set at 80rpm and the temperature setting was 185°C.
- After complete melting of the mixture 4.5g of bis-(hydroxymethyl)-p-cresol, 7.5g of ZnO and 1.5g of stearic acid were added. Mixing was then continued for 2 min at 80rpm, then the mixing speed was reduced to 50rpm for 13 minutes, after which the vulcanizate was discharged, cooled and shredded.
- the shredded vulcanizate was extruded using a HAAKE RHEOMEX R254, IJD 25, single screw extruder, equipped with a conventional PE screw with a compression ratio of 1 :3, and a 3mm rod die.
- the temperature settings were: ZONE 1 : 185°C; ZONE 2:
- ISOPLAST 101 100g of ISOPLAST 101 pellets were dry-blended with 150g nitrile rubber of example 1.
- ISOPLAST 101 is a commercially available rigid TPU from DOW Chemicals, 'ISOPLAST' is a trademark of DOW Chemical Co..
- the T g of this material as measured according to the DSC method described above is about 95°C. The material does not show any major transitions below this temperature.
- the dry mixture was melt-blended in a HAAKE RHEOMIX 3000 internal mixer.
- the mixing rate was set at 80rpm and the temperature setting was 185°C.
- After complete melting of the mixture 6 grams of dicumylperoxide (DCP) was added. Mixing was then continued for 2 min at 80rpm, then the mixing speed was reduced to 50rpm for 13 minutes, after which the vulcanizate was discharged, cooled and shredded.
- DCP dicumylperoxide
- the shredded vulcanizate was extruded using a HAAKE RHEOMEX R254, IJD 25, single screw extruder, equipped with a conventional PE screw with a compression ratio of 1 :3, and a 3mm rod die. Properties of the material were measured on the extruded rods using an Instron 4500, operating with a cross-head speed of 100mm/min. The 13 resulting stress at break of the material was 5.2MPa with an elongation at break of 50% and a Shore A hardness of about 90.
- 100g of the shredded rigid TPU of example 1 was dry-blended with 150g EPDM rubber.(KELTAN 4903, 'KELTAN' is a trademark of DSM). The T g of this rubber was measured by DSC to be about -45°C.
- the dry mixture was melt-blended in a HAAKE RHEOMIX 3000 internal mixer.
- the mixing rate was set at 80rpm and the temperature setting was 185°C.
- DCP dicumylperoxide
- the shredded vulcanizate was extruded using a HAAKE RHEOMEX R254, IJD 25, single screw extruder, equipped with a conventional PE screw with a compression ratio of 1 :3, and a 3mm rod die. Properties of the material were measured on the extruded rods using an Instron 4500, operating with a cross-head speed of 100mm/min. The resulting stress at break of the material was 6.6MPa with an elongation at break of 10% and a Shore A hardness of about 93.
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Abstract
Description
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99907364A EP1053268B1 (en) | 1998-02-09 | 1999-01-13 | Elastomers from compositions comprising rigid thermoplastic polyurethane |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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EP98102213 | 1998-02-09 | ||
EP98102213 | 1998-02-09 | ||
PCT/EP1999/000154 WO1999040137A1 (en) | 1998-02-09 | 1999-01-13 | Elastomers from compositions comprising rigid thermoplastic polyurethane |
EP99907364A EP1053268B1 (en) | 1998-02-09 | 1999-01-13 | Elastomers from compositions comprising rigid thermoplastic polyurethane |
Publications (2)
Publication Number | Publication Date |
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EP1053268A1 true EP1053268A1 (en) | 2000-11-22 |
EP1053268B1 EP1053268B1 (en) | 2002-10-02 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP99907364A Expired - Lifetime EP1053268B1 (en) | 1998-02-09 | 1999-01-13 | Elastomers from compositions comprising rigid thermoplastic polyurethane |
Country Status (20)
Country | Link |
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US (1) | US6291587B1 (en) |
EP (1) | EP1053268B1 (en) |
JP (1) | JP2002502901A (en) |
KR (1) | KR20010040763A (en) |
CN (1) | CN1146605C (en) |
AR (1) | AR014550A1 (en) |
AU (1) | AU762643B2 (en) |
BR (1) | BR9907710A (en) |
CA (1) | CA2318301A1 (en) |
DE (1) | DE69903262T2 (en) |
DK (1) | DK1053268T3 (en) |
ES (1) | ES2186328T3 (en) |
HK (1) | HK1036291A1 (en) |
ID (1) | ID24958A (en) |
MY (1) | MY118416A (en) |
PL (1) | PL342218A1 (en) |
PT (1) | PT1053268E (en) |
TR (1) | TR200002320T2 (en) |
TW (1) | TW518355B (en) |
WO (1) | WO1999040137A1 (en) |
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US6207752B1 (en) * | 1997-12-10 | 2001-03-27 | Advanced Elastomer Systems Lp | Thermoplastic vulcanizates of carboxylated nitrile rubber and thermoplastic polyurethanes |
US6524673B1 (en) * | 1999-05-13 | 2003-02-25 | Jpmorgan Chase Bank | High performance thermoplastic hose and method for manufacturing such hose from a thermoplastic vulcanizate |
BR0013101A (en) * | 1999-08-09 | 2002-04-30 | Huntsman Int Llc | Dynamically vulcanized mixture, process to prepare thermoplastic elastomers, thermoplastic elastomers, and use of mixtures |
TW200600310A (en) * | 2004-06-21 | 2006-01-01 | Microcell Composite Company | High-rate foaming manufacturing method of thermoplastic elastomer composite |
WO2006004698A1 (en) * | 2004-06-29 | 2006-01-12 | Polyone Corporation | Compatibilized thermoplastic elastomer compositions |
RU2397183C2 (en) | 2004-10-12 | 2010-08-20 | Дау Глобал Текнолоджиз Инк. | Alkylacrylate-vinylidene chloride polymer plasticiser |
US7671130B2 (en) * | 2004-12-16 | 2010-03-02 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomers having improved adhesive properties |
US7909194B2 (en) * | 2005-07-01 | 2011-03-22 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcanizates and sealing devices made therewith |
KR100711838B1 (en) | 2005-11-14 | 2007-04-30 | 경상대학교산학협력단 | Thermoplastic elastomer using waste rubber and rubber products manufactured thereby |
JP4897588B2 (en) * | 2006-07-26 | 2012-03-14 | 住友ゴム工業株式会社 | Rubber composition and tire using the same |
AR066616A1 (en) * | 2007-07-27 | 2009-09-02 | Dow Global Technologies Inc | COMPOSITIONS OF THERMOPLASTIC POLYURETHANE (TPU), POLIBUTADIEN AND POLYBIDE BASED TPU |
US20090163663A1 (en) * | 2007-12-19 | 2009-06-25 | Escalator Handrail Company Inc. | Method of preparing thermoplastic polyurethane blends |
CN102782037B (en) | 2009-12-11 | 2014-03-12 | 陶氏环球技术有限责任公司 | Thermoplastic polymer blends comprising dynamically crosslinked polyurethane in olefin polymer matrix |
EP2516496A2 (en) | 2009-12-23 | 2012-10-31 | Epaflex Polyurethanes S.r.l. | One-shot process for the production of thermoplastic polyurethane modified with styrenic block copolymers |
DE102013217661B4 (en) * | 2013-09-04 | 2023-01-12 | Leibniz-Institut Für Polymerforschung Dresden E.V. | Process for producing blends of thermoplastic polyurethanes and rubbers and blends produced therewith |
CN104744920A (en) * | 2013-12-25 | 2015-07-01 | 三晃股份有限公司 | Polymer composite and product and preparation method thereof |
CN104788936A (en) * | 2014-01-16 | 2015-07-22 | 三晃股份有限公司 | Multifunctional environment-friendly polyurethane composite material and preparation method thereof |
CN103788440A (en) * | 2014-02-11 | 2014-05-14 | 太仓市晨洲塑业有限公司 | Improved TPR (Thermoplastic Rubber) formula |
CN105086034A (en) * | 2015-08-26 | 2015-11-25 | 安徽鸿海电缆有限公司 | High-abrasion resistance and high temperature-resistant cable sheath material |
CN109233251A (en) * | 2018-08-29 | 2019-01-18 | 厦门泰启力飞科技有限公司 | Multifunctional natural environment-friendly type polyurethanes polymer composite |
CN112708255A (en) * | 2020-12-24 | 2021-04-27 | 广州机械科学研究院有限公司 | Low-temperature-resistant elastomer rubber composition and application thereof |
CN115073912A (en) * | 2021-03-15 | 2022-09-20 | 彰洋材料股份有限公司 | Thermoplastic vulcanized rubber composition, preparation method thereof and shoe material |
KR102370666B1 (en) * | 2021-03-25 | 2022-03-07 | 의림환경에너텍(주) | Method for manufacturing plastic block with recycled waste wire covering |
EP4063448B1 (en) * | 2021-03-25 | 2023-12-06 | Parker-Hannifin Corporation | Thermoplastic vulcanizates made of thermoplastic polyurethane and carboxylated nitrile butadiene |
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DE2854409A1 (en) * | 1978-12-16 | 1980-06-26 | Bayer Ag | METHOD FOR PRODUCING THERMOPLASTIC CHEMICAL MATERIALS |
US4376834A (en) * | 1981-10-14 | 1983-03-15 | The Upjohn Company | Polyurethane prepared by reaction of an organic polyisocyanate, a chain extender and an isocyanate-reactive material of m.w. 500-20,000 characterized by the use of only 2-25 percent by weight of the latter material |
US4567236A (en) * | 1983-07-18 | 1986-01-28 | The Upjohn Co. | Novel polymer blends |
DE3834103C1 (en) * | 1988-10-07 | 1990-01-18 | Fa. Carl Freudenberg, 6940 Weinheim, De | |
EP0500259A3 (en) * | 1991-02-20 | 1993-01-07 | The Dow Chemical Company | Thermally processable blends of high modulus polyurethanes and impact modifiers |
AU1999192A (en) * | 1991-05-24 | 1992-12-30 | Dow Chemical Company, The | Thermally processable blends of high modulus polyurethanes and mass polymerized abs resins |
DE4126499B4 (en) * | 1991-08-10 | 2004-04-08 | Elastogran Gmbh | Use of polyolefin homo- or copolymers as matting agents for thermoplastic polyurethane elastomers |
EP0769527A1 (en) * | 1995-10-17 | 1997-04-23 | Basf Corporation | Thermoplastic polyurethane compositions exhibiting improved UV and heat resistance |
MX9604747A (en) | 1995-10-17 | 1997-04-30 | Basf Corp | Process for making molded thermoplastic polyurethane articles exhibiting improved uv and heat resistance. |
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1999
- 1999-01-13 WO PCT/EP1999/000154 patent/WO1999040137A1/en not_active Application Discontinuation
- 1999-01-13 CA CA002318301A patent/CA2318301A1/en not_active Abandoned
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- 1999-01-13 PT PT99907364T patent/PT1053268E/en unknown
- 1999-01-13 KR KR1020007008652A patent/KR20010040763A/en not_active Application Discontinuation
- 1999-01-13 DK DK99907364T patent/DK1053268T3/en active
- 1999-01-13 DE DE69903262T patent/DE69903262T2/en not_active Expired - Fee Related
- 1999-01-13 CN CNB998028053A patent/CN1146605C/en not_active Expired - Fee Related
- 1999-01-13 PL PL99342218A patent/PL342218A1/en not_active Application Discontinuation
- 1999-01-13 ES ES99907364T patent/ES2186328T3/en not_active Expired - Lifetime
- 1999-01-13 JP JP2000530563A patent/JP2002502901A/en not_active Withdrawn
- 1999-01-13 EP EP99907364A patent/EP1053268B1/en not_active Expired - Lifetime
- 1999-01-13 ID IDW20001491A patent/ID24958A/en unknown
- 1999-01-13 BR BR9907710-8A patent/BR9907710A/en not_active Application Discontinuation
- 1999-01-13 TR TR2000/02320T patent/TR200002320T2/en unknown
- 1999-01-20 TW TW088100839A patent/TW518355B/en not_active IP Right Cessation
- 1999-02-08 AR ARP990100519A patent/AR014550A1/en unknown
- 1999-02-08 US US09/245,749 patent/US6291587B1/en not_active Expired - Fee Related
- 1999-02-08 MY MYPI99000412A patent/MY118416A/en unknown
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2001
- 2001-09-20 HK HK01106668A patent/HK1036291A1/en not_active IP Right Cessation
Non-Patent Citations (1)
Title |
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See references of WO9940137A1 * |
Also Published As
Publication number | Publication date |
---|---|
BR9907710A (en) | 2000-11-14 |
ID24958A (en) | 2000-08-31 |
DE69903262D1 (en) | 2002-11-07 |
DK1053268T3 (en) | 2003-02-10 |
PT1053268E (en) | 2003-02-28 |
PL342218A1 (en) | 2001-05-21 |
EP1053268B1 (en) | 2002-10-02 |
KR20010040763A (en) | 2001-05-15 |
MY118416A (en) | 2004-10-30 |
CN1146605C (en) | 2004-04-21 |
CN1290276A (en) | 2001-04-04 |
JP2002502901A (en) | 2002-01-29 |
WO1999040137A1 (en) | 1999-08-12 |
TR200002320T2 (en) | 2000-11-21 |
AU2716699A (en) | 1999-08-23 |
AU762643B2 (en) | 2003-07-03 |
CA2318301A1 (en) | 1999-08-12 |
TW518355B (en) | 2003-01-21 |
AR014550A1 (en) | 2001-02-28 |
US6291587B1 (en) | 2001-09-18 |
HK1036291A1 (en) | 2001-12-28 |
ES2186328T3 (en) | 2003-05-01 |
DE69903262T2 (en) | 2003-09-11 |
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